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Cross-talk-dependent cortical patterning of Rho GTPases during cell repair
Rho GTPases such as Rho, Rac, and Cdc42 are important regulators of the cortical cytoskeleton in processes including cell division, locomotion, and repair. In these processes, Rho GTPases assume characteristic patterns wherein the active GTPases occupy mutually exclusive “zones” in the cell cortex....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351735/ https://www.ncbi.nlm.nih.gov/pubmed/34133216 http://dx.doi.org/10.1091/mbc.E20-07-0481 |
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author | Moe, Alison Holmes, William Golding, Adriana E. Zola, Jessica Swider, Zachary T. Edelstein-Keshet, Leah Bement, William |
author_facet | Moe, Alison Holmes, William Golding, Adriana E. Zola, Jessica Swider, Zachary T. Edelstein-Keshet, Leah Bement, William |
author_sort | Moe, Alison |
collection | PubMed |
description | Rho GTPases such as Rho, Rac, and Cdc42 are important regulators of the cortical cytoskeleton in processes including cell division, locomotion, and repair. In these processes, Rho GTPases assume characteristic patterns wherein the active GTPases occupy mutually exclusive “zones” in the cell cortex. During cell wound repair, for example, a Rho zone encircles the wound edge and is in turn encircled by a Cdc42 zone. Here we evaluated the contributions of cross-talk between Rho and Cdc42 to the patterning of their respective zones in wounded Xenopus oocytes using experimental manipulations in combination with mathematical modeling. The results show that the position of the Cdc42 zone relative to the Rho zone and relative to the wound edge is controlled by the level of Rho activity. In contrast, the outer boundary of the Rho zone is limited by the level of Cdc42 activity. Models based on positive feedback within zones and negative feedback from Rho to the GEF-GAP Abr to Cdc42 capture some, but not all, of the observed behaviors. We conclude that GTPase zone positioning is controlled at the level of Rho activity and we speculate that the Cdc42 zone or something associated with it limits the spread of Rho activity. |
format | Online Article Text |
id | pubmed-8351735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-83517352021-10-16 Cross-talk-dependent cortical patterning of Rho GTPases during cell repair Moe, Alison Holmes, William Golding, Adriana E. Zola, Jessica Swider, Zachary T. Edelstein-Keshet, Leah Bement, William Mol Biol Cell Articles Rho GTPases such as Rho, Rac, and Cdc42 are important regulators of the cortical cytoskeleton in processes including cell division, locomotion, and repair. In these processes, Rho GTPases assume characteristic patterns wherein the active GTPases occupy mutually exclusive “zones” in the cell cortex. During cell wound repair, for example, a Rho zone encircles the wound edge and is in turn encircled by a Cdc42 zone. Here we evaluated the contributions of cross-talk between Rho and Cdc42 to the patterning of their respective zones in wounded Xenopus oocytes using experimental manipulations in combination with mathematical modeling. The results show that the position of the Cdc42 zone relative to the Rho zone and relative to the wound edge is controlled by the level of Rho activity. In contrast, the outer boundary of the Rho zone is limited by the level of Cdc42 activity. Models based on positive feedback within zones and negative feedback from Rho to the GEF-GAP Abr to Cdc42 capture some, but not all, of the observed behaviors. We conclude that GTPase zone positioning is controlled at the level of Rho activity and we speculate that the Cdc42 zone or something associated with it limits the spread of Rho activity. The American Society for Cell Biology 2021-08-01 /pmc/articles/PMC8351735/ /pubmed/34133216 http://dx.doi.org/10.1091/mbc.E20-07-0481 Text en © 2021 Moe et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/3.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License. |
spellingShingle | Articles Moe, Alison Holmes, William Golding, Adriana E. Zola, Jessica Swider, Zachary T. Edelstein-Keshet, Leah Bement, William Cross-talk-dependent cortical patterning of Rho GTPases during cell repair |
title | Cross-talk-dependent cortical patterning of Rho GTPases during cell repair |
title_full | Cross-talk-dependent cortical patterning of Rho GTPases during cell repair |
title_fullStr | Cross-talk-dependent cortical patterning of Rho GTPases during cell repair |
title_full_unstemmed | Cross-talk-dependent cortical patterning of Rho GTPases during cell repair |
title_short | Cross-talk-dependent cortical patterning of Rho GTPases during cell repair |
title_sort | cross-talk-dependent cortical patterning of rho gtpases during cell repair |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351735/ https://www.ncbi.nlm.nih.gov/pubmed/34133216 http://dx.doi.org/10.1091/mbc.E20-07-0481 |
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